EP3056487B1 - Synthèse d'un intermédiaire de l'énone - Google Patents

Synthèse d'un intermédiaire de l'énone Download PDF

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EP3056487B1
EP3056487B1 EP15200282.0A EP15200282A EP3056487B1 EP 3056487 B1 EP3056487 B1 EP 3056487B1 EP 15200282 A EP15200282 A EP 15200282A EP 3056487 B1 EP3056487 B1 EP 3056487B1
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hydrogen
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EP3056487A1 (fr
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Andrew G Myers
Jason D Brubaker
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Harvard College
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D231/18—One oxygen or sulfur atom
    • C07D231/20—One oxygen atom attached in position 3 or 5
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/24—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring of the carbon skeleton
    • C07C237/26—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring of the carbon skeleton of a ring being part of a condensed ring system formed by at least four rings, e.g. tetracycline
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
    • C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D261/12—Oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/20—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings condensed with carbocyclic rings or ring systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
    • C07D498/18—Bridged systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804—Compounds having Si-O-C linkages
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804—Compounds having Si-O-C linkages
    • C07F7/1872—Preparation; Treatments not provided for in C07F7/20
    • C07F7/1892—Preparation; Treatments not provided for in C07F7/20 by reactions not provided for in C07F7/1876 - C07F7/1888

Definitions

  • the tetracyclines are broad spectrum anti-microbial agents that are widely used in human and veterinary medicine ( Schappinger et al., "Tetracyclines: Antibiotic Action, Uptake, and Resistance Mechanisms” Arch. Microbiol. 165:359-69, 1996 ; Mitscher, Medicinal Research Series, Vol. 9, The Chemistry of the Tetracycline Antibiotics, Marcel Dekker Inc. New York, 1978 ).
  • the total production of tetracyclines by fermentation or semi-synthesis is measured in the thousands of metric tons per year.
  • chlorotetracycline (1) (AureomycinTM) was isolated from the soil bacterium Streptomyces aureofaciens by Lederle Laboratories (Wyeth-Ayerst Research) in the 1945 ( Duggar, Ann. N.Y. Acad. Sci. 51:177-181, 1948 ; Duggar, Aureomycin and Preparation of Some, U.S. Patent 2,482,055, 1949 ).
  • Oxytetracycline (2) was isolated soon after from S. rimosus by scientists at Pfizer Laboratories ( Finlay et al. Science 111:85, 1950 ).
  • Tetracycline (3) was later prepared by the hydrogenolysis of chlorotetracycline and was found to retain the anti-microbial activity of chlorotetracycline and oxytetracycline and had increased stability ( Boothe et al. J. Am. Chem. Soc. 75:4621, 1953 ; Conover et al. J. Am. Chem. Soc. 75:4622-23, 1953 ). Tetracycline was later found to be a natural product of S. aureofaciens, S. viridofaciens, and S. rimosus.
  • the primary tetracyclines of clinical importance today include tetracycline (3) ( Boothe et al. J. Am. Chem. Soc. 75:4621, 1953 ), oxytetracycline ( 2 , TerramycinTM) ( Finlay et al. Science 111:85, 1950 ), (-)-doxycycline ( Stephens et al. J. Am. Chem. Soc. 85:2643, 1963 ), (-)-minocycline ( Martell et al. J. Med. Chem. 10:44, 1967 ; Martell et al. J. Med. Chem. 10:359, 1967 ), and tigecycline.
  • the tetracyclines exert their anti-microbial activity by inhibition of bacterial protein synthesis ( Bentley and O'Hanlon, Eds., Anti-Infectives: Recent Advances in Chemistry and Structure-Activity Relationships The Royal Society of Chemistry: Cambridge, UK, 1997 ). Most tetracyclines are bacteriostatic rather than bactericidal ( Rasmussen et al. Antimicrob. Agents Chemother. 35:2306-11, 1991 ; Primrose and Wardlaw, Ed. "The Bacteriostatic and Bacteriocidal Action of Antibiotics" Sourcebook of Experiments for the Teaching of Microbiology Society for General Microbiology, Academic Press Ltd., London, 1982 ).
  • Tetracyclines have also been found to bind to the 40S subunit of eukaryotic ribosome; however, they do not achieve sufficient concentrations in eukaryotic cells to affect protein synthesis because they are not actively transported in eukaryotic cells ( Epe et al. FEBS Lett. 213:443-47, 1987 ).
  • the tetracyclines are composed of four linearly fused six-membered rings with a high density of polar functionality and stereochemical complexity. Previous approaches to the synthesis of tetracyclines typically proceeded via a stepwise assembly of the tetracyclic ring system. In 1962, Woodward and co-workers reported the first total synthesis of racemic 6-desmethyl-6-deoxytetracycline (sancycline, 4 ), the simplest biologically active tetracycline ( Conover et al. J. Am. Chem. Soc. 84:3222-24, 1962 ). The synthetic route was a remarkable achievement for the time and proceeded by the stepwise construction of the rings in a linear sequence of 22 steps (overall yield ⁇ 0.003%).
  • the first approach involves the reaction of the enone with an anion formed by the deprotonation of a toluate (6) or metallation of a benzylic halide as shown below.
  • a second approach involves reacting the enone in a Diels-Alder-type reaction with a diene (7) or a benzocyclobutenol (8).
  • the chiral enone provides the functionalized A and B rings of the tetracycline core, and the D-ring is derived from the toluate (6), benzylic halide, or benzocyclobutenol (8).
  • the C-ring is formed, preferably in a stereoselective manner.
  • enone of formula 9 One exemplary synthesis of an enone of formula 9 is shown below.
  • the synthesis begins with aldehyde 10 and in eight steps yields enone 18.
  • Aldehyde 10 is coupled with a vinyl reagent to yield a mixture of enantiomers of the corresponding alcohol.
  • Chiral resolution using amano lipase followed by substitution yields compound 13, which is subsequently metalated and reacted with 3-methoxyfurfural.
  • the allylic alcohol may be prepared by enantioselective addition of the vinyl group to the aldehyde 10. Intramolecular cyclization of 14 yields the bridged tricycle 15.
  • the coupling of the isoxazole to 3-methyoxyfurfural to prepare compound 14 may be achieved by a metal-halogen exhange reaction, rather than low-temperature metalation, using a derivative of 13 of the formula: wherein X is a halgoen ( e.g. , iodine or bromine).
  • X is a halgoen (e.g. , iodine or bromine).
  • the present invention includes individual steps (e.g. , reduction, protection, deprotection, chiral resolution, metalation, rearrangment, de-methylation, etc .) in the synthesis of an enone of formula 9 as well as any combination of steps in the synthetic scheme.
  • the inventive synthesis allows for the production of multi-gram quantitities of the final product.
  • the synthesis may provide at least 50 g of the desired enone.
  • Particularly useful intermediates in the synthetic scheme leading to enones of the formula 18 may be provided.
  • Particularly useful intermediates include compounds of the formula: or salts, stereoisomers, enantiomers, diastereomers, tautomers, or protected or unprotected forms of the intermediates.
  • the various intermediates with chiral centers are provided in enantiomeric or diasteroemeric pure form or are provided as a mixture of stereoisomers.
  • the present invention also provides the synthesis of tetracycline anlogs using the synthetic methodology for preparing the enone (9), described herein.
  • a chiral enone (9) prepared by the methodology described herein is used in combination with the methodologies described in US 2005/0292787 to prepare a tetracycline analog.
  • the inventive synthesis of the enone intermediate may be used to synthesize any compound described in U.S. patent application, US2005/0282787, published December 22, 2005 ; international PCT application, WO 05/112945, published December 1, 2005 ; U.S. provisional patent application, U.S.S.N.
  • inventive methods and intermediates may also be used to prepare tetracyclines or tetracycline analogs known in the art (e.g., doxycycline, sancycline, minocycline, tigecycline, tetracycline, etc .) .
  • the new synthetic approach to the enone intermediate is particularly useful in preparing 6-deoxytetracyclines.
  • the new synthetic methodology and intermediates are also useful in preparing 6-hydroxytetracyclines, pentacyclines, hexacyclines, C5-substituted tetracyclines, C5-unsubstituted tetracyclines, tetracyclines with heterocyclic D-rings, and other tetracycline analogs.
  • the new synthesis of enone (9) is also useful in preparing other organic compounds which may or may not be related to tetracyclines.
  • the invention provides several basic approaches to the synthesis of tetracycline analogs using the synthesis described herein for preparing the enone intermediate.
  • the first approach to preparing tetracycline analogs involves reaction of the enone with an anion formed by the deprotonation of a toluate .
  • the deprotonation of a toluate is particularly useful in preparing 6-deoxytetracyclines with or without a C5-substituent.
  • the chiral enone provides the functionalized A and B rings of the tetracycline core, and the D-ring is derived from the toluate. In bringing these two portions of the molecule together the C-ring is formed.
  • the C-ring is formed in a stereoselective manner.
  • This approach not only allows for the stereoselective and efficient synthesis of a wide variety of tetracycline analogs, but also for the efficient preparation of tetracycline analogs in which the D-ring is replaced with a heterocycle, 5-membered ring, or other ring system.
  • This approach also allows the prepartion of various pentacyclines or higher cyclines containing aromatic and non-aromatic carbocycles and heterocycles.
  • This approach also allows for the preparation of various tricyclines.
  • the inventive intermediates may have biological activity.
  • an intermediate may possess anti-microbial or anti-proliferative activity.
  • the present invention provides pharmaceutical compositions including the novel compounds of the present invention for use in therapy.
  • the pharmaceutical compositions may optionally include a pharmaceutically acceptable excipient.
  • the pharmaceutical compositions may be used to treat any infection including cholera, influenza, bronchitis, acne, malaria, urinary tract infections, sexually transmitted diseases including syphilis and gonorrhea, Legionnaires' disease, Lyme disease, Rocky Mountain spotted fever, Q fever, typhus, bubonic plague, gas gangrene, hospital acquired infections, leptospirosis, whooping cough, and anthrax.
  • the infections are caused by tetracycline-resistant organisms.
  • the compounds of the invention exhibit anti-neoplastic or anti-proliferative activity, in which case the compounds may be useful in the treatment of diseases such as cancer, autoimmune diseases, inflammatory diseases, and diabetic retinopathy.
  • the compositions may be used to treat disease in humans and other animals including domesticated animals. Any mode of administration including oral and parenteral administration of a pharmaceutical composition comprising an inventive compound may be used.
  • the present invention represents an improvement in the overall synthetic approach to tetracycline analogs.
  • the present invention allows for the preparation of tetracycline analogs in higher yields than previously attainable.
  • the new synthetic approach to the enone intermediate also makes the synthesis of tetracycline analogs more amenable to large-scale production given its improved overall yield.
  • Certain compounds of the present invention may exist in particular geometric or stereoisomeric forms.
  • the present invention contemplates all such compounds, including cis- and trans -isomers, E- and Z -isomers, R- and S -enantiomers, diastereomers, (D)-isomers, (L)-isomers, (-)- and (+)-isomers, racemic mixtures thereof, and other mixtures thereof, as falling within the scope of the invention.
  • Additional asymmetric carbon atoms may be present in a substituent such as an aliphatic ( e.g ., alkyl) or heteroaliphatic group. All such isomers, as well as mixtures thereof, are considered to be within this invention.
  • Isomeric mixtures containing any of a variety of isomer ratios may be utilized in accordance with the present invention. For example, where only two isomers are combined, mixtures containing 50:50, 60:40, 70:30, 80:20, 90:10, 95:5, 96:4, 97:3, 98:2, 99:1, or 100:0 isomer ratios are all contemplated by the present invention. Those of ordinary skill in the art will readily appreciate that analogous ratios are contemplated for more complex isomer mixtures.
  • a particular enantiomer of a compound of the present invention may be prepared by asymmetric synthesis, or by derivation with a chiral auxiliary, where the resulting diastereomeric mixture is separated and the auxiliary group cleaved to provide the pure desired enantiomers.
  • the molecule contains a basic functional group, such as amino, or an acidic functional group, such as carboxyl, diastereomeric salts are formed with an appropriate optically-active acid or base, followed by resolution of the diastereomers thus formed by fractional crystallization or chromatographic means known in the art, and subsequent recovery of the pure enantiomers.
  • protecting group it is meant that a particular functional moiety, e.g., O, S, or N, is temporarily blocked so that a reaction can be carried out selectively at another reactive site in a multifunctional compound.
  • a protecting group reacts selectively in good yield to give a protected substrate that is stable to the projected reactions; the protecting group should be selectively removable in good yield by readily available, preferably non-toxic reagents that do not attack the other functional groups; the protecting group forms an easily separable derivative (more preferably without the generation of new stereogenic centers); and the protecting group has a minimum of additional functionality to avoid further sites of reaction.
  • oxygen, sulfur, nitrogen, and carbon protecting groups may be utilized.
  • Hydroxyl protecting groups include methyl, methoxylmethyl (MOM), methylthiomethyl (MTM), t -butylthiomethyl, (phenyldimethylsilyl)methoxymethyl (SMOM), benzyloxymethyl (BOM), p- methoxybenzyloxymethyl (PMBM), (4-methoxyphenoxy)methyl ( p -AOM), guaiacolmethyl (GUM), t -butoxymethyl, 4-pentenyloxymethyl (POM), siloxymethyl, 2-methoxyethoxymethyl (MEM), 2,2,2-trichloroethoxymethyl, bis(2-chloroethoxy)methyl, 2-(trimethylsilyl)ethoxymethyl (SEMOR), tetrahydropyranyl (THP), 3-bromotetrahydropyranyl, tetrahydrothiopyranyl, 1-methoxycyclohexyl, 4-methoxytetrahydropyranyl (MTHP), 4-methoxy
  • the protecting groups include methylene acetal, ethylidene acetal, 1- t -butylethylidene ketal, 1-phenylethylidene ketal, (4-methoxyphenyl)ethylidene acetal, 2,2,2-trichloroethylidene acetal, acetonide, cyclopentylidene ketal, cyclohexylidene ketal, cycloheptylidene ketal, benzylidene acetal, p- methoxybenzylidene acetal, 2,4-dimethoxybenzylidene ketal, 3,4-dimethoxybenzylidene acetal, 2-nitrobenzylidene acetal, methoxymethylene acetal, ethoxymethylene acetal, dimethoxymethylene ortho ester, 1-methoxyethylidene ortho este
  • Amino-protecting groups include methyl carbamate, ethyl carbamante, 9-fluorenylmethyl carbamate (Fmoc), 9-(2-sulfo)fluorenylmethyl carbamate, 9-(2,7-dibromo)fluoroenylmethyl carbamate, 2,7-di- t -butyl-[9-(10,10-dioxo-10,10,10,10-tetrahydrothioxanthyl)]methyl carbamate (DBD-Tmoc), 4-methoxyphenacyl carbamate (Phenoc), 2,2,2-trichloroethyl carbamate (Troc), 2-trimethylsilylethyl carbamate (Teoc), 2-phenylethyl carbamate (hZ), 1-(1-adamantyl)-1-methylethyl carbamate (Adpoc), 1,1-dimethyl-2-haloethyl carbamate, 1,1
  • protecting groups are detailed herein, however, it will be appreciated that the present invention is not intended to be limited to these protecting groups; rather, a variety of additional equivalent protecting groups can be readily identified using the above criteria and utilized in the method of the present invention. Additionally, a variety of protecting groups are described in Protective Groups in Organic Synthesis, Third Ed. Greene, T.W. and Wuts, P.G., Eds., John Wiley & Sons, New York: 1999 .
  • the compounds, as described herein, may be substituted with any number of substituents or functional moieties.
  • substituted refers to the replacement of hydrogen radicals in a given structure with the radical of a specified substituent.
  • only one hydrogen radical in a given structure is replaced with the radical of a specified substituent.
  • one, two, or three hydrogen radicals in a given structure are replaced with the same or different radicals of a specified substituent.
  • the substituent may be either the same or different at every position.
  • the term "substituted" is contemplated to include all permissible substituents of organic compounds.
  • the permissible substituents include acyclic and cyclic, branched and unbranched, carbocyclic and heterocyclic, aromatic and nonaromatic substituents of organic compounds.
  • heteroatoms such as nitrogen may have hydrogen substituents and/or any permissible substituents of organic compounds described herein which satisfy the valencies of the heteroatoms.
  • this invention is not intended to be limited in any manner by the permissible substituents of organic compounds.
  • Combinations of substituents and variables envisioned by this invention are preferably those that result in the formation of stable compounds useful in the treatment, for example, of infectious diseases or proliferative disorders.
  • stable preferably refers to compounds which possess stability sufficient to allow manufacture and which maintain the integrity of the compound for a sufficient period of time to be detected and preferably for a sufficient period of time to be useful for the purposes detailed herein.
  • aliphatic includes both saturated and unsaturated, straight chain ( i.e., unbranched), branched, acyclic, cyclic, or polycyclic aliphatic hydrocarbons, which are optionally substituted with one or more functional groups.
  • aliphatic is intended herein to include, but is not limited to, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, and cycloalkynyl moieties.
  • alkyl includes straight, branched and cyclic alkyl groups.
  • alkyl alkenyl
  • alkynyl alkynyl
  • lower alkyl is used to indicate those alkyl groups (cyclic, acyclic, substituted, unsubstituted, branched or unbranched) having 1-6 carbon atoms.
  • the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-20 aliphatic carbon atoms. In certain other embodiments, the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-10 aliphatic carbon atoms. In yet other embodiments, the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-8 aliphatic carbon atoms. In still other embodiments, the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-6 aliphatic carbon atoms. In yet other embodiments, the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-4 carbon atoms.
  • Illustrative aliphatic groups thus include, but are not limited to, for example, methyl, ethyl, n-propyl, isopropyl, cyclopropyl, -CH 2 -cyclopropyl, vinyl, allyl, n-butyl, sec-butyl, isobutyl, tert-butyl, cyclobutyl, -CH 2 -cyclobutyl, n-pentyl, sec-pentyl, isopentyl, tert-pentyl, cyclopentyl, -CH 2 -cyclopentyl, n-hexyl, sec-hexyl, cyclohexyl, -CH 2 -cyclohexyl moieties and the like, which again, may bear one or more substituents.
  • Alkenyl groups include, but are not limited to, for example, ethenyl, propenyl, butenyl, 1-methyl-2-buten-1-yl, and the like.
  • Representative alkynyl groups include, but are not limited to, ethynyl, 2-propynyl (propargyl), 1-propynyl, and the like.
  • alkoxy refers to an alkyl group, as previously defined, attached to the parent molecule through an oxygen atom or through a sulfur atom.
  • the alkyl, alkenyl, and alkynyl groups contain 1-20 alipahtic carbon atoms.
  • the alkyl, alkenyl, and alkynyl groups contain 1-10 aliphatic carbon atoms.
  • the alkyl, alkenyl, and alkynyl groups employed in the invention contain 1-8 aliphatic carbon atoms.
  • the alkyl, alkenyl, and alkynyl groups contain 1-6 aliphatic carbon atoms. In yet other embodiments, the alkyl, alkenyl, and alkynyl groups contain 1-4 aliphatic carbon atoms.
  • alkoxy include but are not limited to, methoxy, ethoxy, propoxy, isopropoxy, n-butoxy, tert-butoxy, neopentoxy, and n-hexoxy.
  • Examples of thioalkyl include, but are not limited to, methylthio, ethylthio, propylthio, isopropylthio, n-butylthio, and the like.
  • alkylamino refers to a group having the structure -NHR', wherein R' is aliphatic, as defined herein.
  • the aliphatic group contains 1-20 aliphatic carbon atoms.
  • the aliphatic group contains 1-10 aliphatic carbon atoms.
  • the aliphatic group employed in the invention contain 1-8 aliphatic carbon atoms.
  • the aliphatic group contains 1-6 aliphatic carbon atoms.
  • the aliphatic group contains 1-4 aliphatic carbon atoms.
  • alkylamino groups include, but are not limited to, methylamino, ethylamino, n-propylamino, iso-propylamino, cyclopropylamino, n-butylamino, tert-butylamino, neopentylamino, n-pentylamino, hexylamino, cyclohexylamino, and the like.
  • dialkylamino refers to a group having the structure -NRR', wherein R and R' are each an aliphatic group, as defined herein. R and R' may be the same or different in an dialkyamino moiety.
  • the aliphatic groups contains 1-20 aliphatic carbon atoms. In certain other embodiments, the aliphatic groups contains 1-10 aliphatic carbon atoms. In yet other embodiments, the aliphatic groups employed in the invention contain 1-8 aliphatic carbon atoms. In still other embodiments, the aliphatic groups contains 1-6 aliphatic carbon atoms. In yet other embodiments, the aliphatic groups contains 1-4 aliphatic carbon atoms.
  • dialkylamino groups include, but are not limited to, dimethylamino, methyl ethylamino, diethylamino, methylpropylamino, di(n-propyl)amino, di(iso-propyl)amino, di(cyclopropyl)amino, di(n-butyl)amino, di(tert-butyl)amino, di(neopentyl)amino, di(n-pentyl)amino, di(hexyl)amino, di(cyclohexyl)amino, and the like.
  • R and R' are linked to form a cyclic structure.
  • cyclic structure may be aromatic or non-aromatic.
  • cyclic diaminoalkyl groups include, but are not limted to, aziridinyl, pyrrolidinyl, piperidinyl, morpholinyl, pyrrolyl, imidazolyl, 1,3,4-trianolyl, and tetrazolyl.
  • substituents of the above-described aliphatic (and other) moieties of compounds of the invention include, but are not limited to aliphatic; heteroaliphatic; aryl; heteroaryl; arylalkyl; heteroarylalkyl; alkoxy; aryloxy; heteroalkoxy; heteroaryloxy; alkylthio; arylthio; heteroalkylthio; heteroarylthio; F; Cl; Br; I; -OH; -NO 2 ;-CN; -CF 3 ; -CH 2 CF 3 ; -CHCl 2 ; -CH 2 OH; -CH 2 CH 2 OH; -CH 2 NH 2 ; -CH 2 SO 2 CH 3 ; -C(O)R x ;-CO 2 (R x ); -CON(R x ) 2 ; -OC(O)R x ; -OCO 2 R x ; -OCON(R x ) 2
  • aryl and heteroaryl refer to stable mono- or polycyclic, heterocyclic, polycyclic, and polyheterocyclic unsaturated moieties having preferably 3-14 carbon atoms, each of which may be substituted or unsubstituted.
  • Substituents include, but are not limited to, any of the previously mentioned substitutents, i.e., the substituents recited for aliphatic moieties, or for other moieties as disclosed herein, resulting in the formation of a stable compound.
  • aryl refers to a mono- or bicyclic carbocyclic ring system having one or two aromatic rings including, but not limited to, phenyl, naphthyl, tetrahydronaphthyl, indanyl, indenyl, and the like.
  • heteroaryl refers to a cyclic aromatic radical having from five to ten ring atoms of which one ring atom is selected from S, O, and N; zero, one, or two ring atoms are additional heteroatoms independently selected from S, O, and N; and the remaining ring atoms are carbon, the radical being joined to the rest of the molecule via any of the ring atoms, such as, for example, pyridyl, pyrazinyl, pyrimidinyl, pyrrolyl, pyrazolyl, imidazolyl, thiazolyl, oxazolyl, isooxazolyl, thiadiazolyl,oxadiazolyl, thiophenyl, furanyl, quinolinyl, isoquinolinyl, and the like.
  • aryl and heteroaryl groups can be unsubstituted or substituted, wherein substitution includes replacement of one, two, three, or more of the hydrogen atoms thereon independently with any one or more of the following moieties including, but not limited to: aliphatic; heteroaliphatic; aryl; heteroaryl; arylalkyl; heteroarylalkyl; alkoxy; aryloxy; heteroalkoxy; heteroaryloxy; alkylthio; arylthio; heteroalkylthio; heteroarylthio; -F; -Cl; -Br; -I; -OH; -NO 2 ; -CN; -CF 3 ; -CH 2 CF 3 ; -CHCl 2 ;-CH 2 OH; -CH 2 CH 2 OH; -CH 2 NH 2 ; -CH 2 SO 2 CH 3 ; -C(O)R x ; -CO 2 (R x ); -CON
  • cycloalkyl refers specifically to groups having three to seven, preferably three to ten carbon atoms. Suitable cycloalkyls include, but are not limited to cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and the like, which, as in the case of other aliphatic, heteroaliphatic, or hetercyclic moieties, may optionally be substituted with substituents including, but not limited to aliphatic; heteroaliphatic; aryl; heteroaryl; arylalkyl; heteroarylalkyl; alkoxy; aryloxy; heteroalkoxy; heteroaryloxy; alkylthio; arylthio; heteroalkylthio; heteroarylthio; -F; -Cl; -Br; -I; -OH; -NO 2 ; -CN; -CF 3 ;-CH 2 CF 3
  • heteroaliphatic refers to aliphatic moieties that contain one or more oxygen, sulfur, nitrogen, phosphorus, or silicon atoms, e.g., in place of carbon atoms. Heteroaliphatic moieties may be branched, unbranched, cyclic or acyclic and include saturated and unsaturated heterocycles such as morpholino, pyrrolidinyl, etc.
  • heteroaliphatic moieties are substituted by independent replacement of one or more of the hydrogen atoms thereon with one or more moieties including, but not limited to aliphatic; heteroaliphatic; aryl; heteroaryl; arylalkyl; heteroarylalkyl; alkoxy; aryloxy; heteroalkoxy; heteroaryloxy; alkylthio; arylthio; heteroalkylthio; heteroarylthio; -F;-Cl; -Br; -I; -OH; -NO 2 ; -CN; -CF 3 ; -CH 2 CF 3 ; -CHCl 2 ; -CH 2 OH; -CH 2 CH 2 OH; -CH 2 NH 2 ;-CH 2 SO 2 CH 3 ; -C(O)R x ; -CO 2 (R x ); -CON(R x ) 2 ; -OC(O)R x ; -OCO
  • haloalkyl denotes an alkyl group, as defined above, having one, two, or three halogen atoms attached thereto and is exemplified by such groups as chloromethyl, bromoethyl, trifluoromethyl, and the like.
  • heterocycloalkyl refers to a non-aromatic 5-, 6-, or 7- membered ring or a polycyclic group, including, but not limited to a bi- or tri-cyclic group comprising fused six-membered rings having between one and three heteroatoms independently selected from oxygen, sulfur and nitrogen, wherein (i) each 5-membered ring has 0 to 1 double bonds and each 6-membered ring has 0 to 2 double bonds, (ii) the nitrogen and sulfur heteroatoms may be optionally be oxidized, (iii) the nitrogen heteroatom may optionally be quaternized, and (iv) any of the above heterocyclic rings may be fused to a benzene ring.
  • heterocycles include, but are not limited to, pyrrolidinyl, pyrazolinyl, pyrazolidinyl, imidazolinyl, imidazolidinyl, piperidinyl, piperazinyl, oxazolidinyl, isoxazolidinyl, morpholinyl, thiazolidinyl, isothiazolidinyl, and tetrahydrofuryl.
  • a "substituted heterocycloalkyl or heterocycle” group refers to a heterocycloalkyl or heterocycle group, as defined above, substituted by the independent replacement of one, two or three of the hydrogen atoms thereon with but are not limited to aliphatic; heteroaliphatic; aryl; heteroaryl; arylalkyl; heteroarylalkyl; alkoxy; aryloxy; heteroalkoxy; heteroaryloxy; alkylthio; arylthio; heteroalkylthio; heteroarylthio; -F; -Cl; -Br; -I; -OH; -NO 2 ; -CN; -CF 3 ; -CH 2 CF 3 ; -CHCl 2 ;-CH 2 OH; -CH 2 CH 2 OH; -CH 2 NH 2 ; -CH 2 SO 2 CH 3 ; -C(O)R x ;
  • Carbocycle refers to an aromatic or non-aromatic ring in which each atom of the ring is a carbon atom.
  • label As used herein, the term “labeled” is intended to mean that a compound has at least one element, isotope, or chemical compound attached to enable the detection of the compound.
  • labels typically fall into three classes: a) isotopic labels, which may be radioactive or heavy isotopes, including, but not limited to, 2 H, 3 H, 32 P, 35 S, 67 Ga, 99m Tc (Tc-99m), 111 In, 123 I, 125 I, 169 Yb, and 186 Re; b) immune labels, which may be antibodies or antigens,which may be bound to enzymes (such as horseradish peroxidase) that produce detectable agents; and c) colored, luminescent, phosphorescent, or fluorescent dyes.
  • isotopic labels which may be radioactive or heavy isotopes, including, but not limited to, 2 H, 3 H, 32 P, 35 S, 67 Ga, 99m Tc (Tc-99m), 111 In, 123 I, 125
  • the labels may be incorporated into the compound at any position that does not interfere with the biological activity or characteristic of the compound that is being detected.
  • hydrogen atoms in the compound are replaced with deuterium atoms ( 2 H) to slow the degradation of compound in vivo. Due to isotope effects, enzymatic degradation of the deuterated tetracyclines may be slowed thereby increasing the half-life of the compound in vivo.
  • photoaffinity labeling is utilized for the direct elucidation of intermolecular interactions in biological systems.
  • photophores can be employed, most relying on photoconversion of diazo compounds, azides, or diazirines to nitrenes or carbenes ( see Bayley, H., Photogenerated Reagents in Biochemistry and Molecular Biology (1983), Elsevier, Amsterd am.).
  • the photoaffinity labels employed are o-, m- and p-azidobenzoyls, substituted with one or more halogen moieties, including, but not limited to 4-azido-2,3,5,6-tetrafluorobenzoic acid.
  • Tautomers are particular isomers of a compound in which a hydrogen and double bond have changed position with respect to the other atoms of the molecule. For a pair of tautomers to exist there must be a mechanism for interconversion. Examples of tautomers include keto-enol forms, imine-enamine forms, amide-imino alcohol forms, amidine-aminidine forms, nitroso-oxime forms, thio ketone-enethiol forms, N -nitroso-hydroxyazo forms, nitro- aci -nitro forms, and pyridione-hydroxypyridine forms.
  • Animal refers to humans as well as non-human animals, including, for example, mammals, birds, reptiles, amphibians, and fish. Any animal may be administered a tetracycline analog for the treatment of disease.
  • the non-human animal is a mammal (e.g ., a rodent, a mouse, a rat, a rabbit, a monkey, a dog, a cat, a primate, or a pig).
  • a non-human animal may be a transgenic animal. In certain embodiments, the animal is human.
  • association When two entities are “associated with” one another as described herein, they are linked by a direct or indirect covalent or non-covalent interaction. Preferably, the association is covalent. Desirable non-covalent interactions include hydrogen bonding, van der Waals interactions, hydrophobic interactions, magnetic interactions, electrostatic interactions, etc.
  • the effective amount of an active agent or the microparticles refers to an amount sufficient to elicit the desired biological response.
  • the effective amount of a compound of the invention may vary depending on such factors as the desired biological endpoint, the pharmacokinetics of the compound, the disease being treated, the mode of administration, and the patient.
  • the effective amount of a tetracycline analog antibiotic is the amount that results in a sufficient concentration at the site of the infection to kill the microorganism causing the infection (bacteriocidal) or to inhibit the reproduction of such microorganisms (bacteriostatic).
  • the effective amount of tetracycline analog antibiotic is the amount sufficient to reverse clinicals signs and symptoms of the infection, including fever, redness, warmth, pain, chills, cultures, and pus production.
  • Tetracycline analog The term, "tetracycline analog,” as referred to herein refers to any compound prepared using the inventive methodology. Tetracycline analogs are typically compounds that can be prepared using the enone (9) as an intermediate in the synthesis. Tetracycline analogs include dicylines, tricyclines, tetracyclines, pentacyclines, hexacyclines, or higher. In certain embodiments, the ring system may contain heterocycles. In certain embodiments, the ring system may contain three-membered rings, four-membered rings, five-membered rings, six-membered rings, seven-membered rings, or higher.
  • the tetracycline analogs is a 6-deoxytetracyline. In other embodiments, the tetracycline analog is a 6-hydroxytetracycline. In other embodiments, the tetracycline analog is a pentacycline. In other embodiments, the tetracycline analog is a C5-substituted tetracycline. In yet other embodiments, the tetracycline analog is a C5-unsubstituted tetracycline. In certain embodiments, the tetracycline analogs have biological activity such as anti-microbial activity or anti-proliferative activity.
  • the present invention provides a method of preparing a compound of or a salt, tautomer, stereoisomer, enantiomer, or diastereomer thereof; wherein:
  • the present invention provides all steps, methodologies, intermediates, and reagents useful in preparing the enone (9) along the synthetic route.
  • the present invention provides for use of this methodology in the modular synthesis of tetracycline analogs by joining the highly functionalized chiral enone, which will become the A- and B-rings of the tetracycline core, with a molecule which will become the D-ring of the tetracycline core.
  • the joining of these two intermediates results in the formation of the C-ring, preferably in an enantioselective manner.
  • This methodology also allows for the synthesis of pentacyclines, hexacyclines, or higher ring systems as well as the incorporation of heterocycles into the ring system.
  • the joining of these two fragments includes various nucleophilic addition reactions and cycloaddition reactions with enone (9) as described above and in U.S. patent application US2005/0282787, published December 22, 2005 .
  • the synthesis of enone (9) begins with the aldehyde (10).
  • the aldehyde moiety is reduced by the addition of a vinyl moiety or substituted vinyl moiety.
  • the addition of the vinyl moiety is accomplished with any vinyl reagent.
  • a metal vinyl reagent is used in the reaction.
  • the metal vinyl reagent is of the formula: wherein
  • the reduction step is stereoselective yielding only one or substantially one enantiomer.
  • the enantioselective reaction results in an an enantiomeric excess (ee) of at least 80%, at least 90%, at least 95%, at least 98%, or at least 99%.
  • the addition of the vinyl moiety is acid catalyzed, for example, Lewis acid catalyzed.
  • a Grignard reagent is used in the reaction.
  • a vinyl lithium reagent is used in the reaction.
  • a vinyl zinc reagent is used in the reaction.
  • the reduction step is enantioselective by addition of divinyl zinc with a chiral ligand.
  • the chiral ligand used is an amino-alcohol ligand of formula: wherein each occurrence of R is independently hydrogen; halogen; cyclic or acyclic, substituted or unsubstituted, branched or unbranched aliphatic; cyclic or acyclic, substituted or unsubstituted, branched or unbranched heteroaliphatic; substituted or unsubstituted, branched or unbranched acyl; substituted or unsubstituted, branched or unbranched aryl; or substituted or unsubstituted, branched or unbranched heteroaryl; and the two occurrences of R may optionally form a heterocyclic moiety.
  • each occurrence of R is hydrogen or C 1 -C 6 alkyl. In certain embodiments, each occurrence of R is C 1 -C 6 alkyl. In certain embodiments, the two occurrences of R for a heterocyclic moiety. In certain embodiments, both R are methyl. In certain embodimments, NR 2 forms a pyrrolidine moiety. In certain embodiments, the two occurrences of R for a heteroaryl moiety. In certain embodiments, the chiral ligand used is an amino-alcohol ligand of formula:
  • the aldehyde 10 is reduced by a metal reagent with a moiety that is subsequently converted into a alkenyl group as show in compound 11.
  • the alkenyl moiety may result from an elimination reaction, reduction of an alkyne, deoxygenation of an epoxide, Wittig-type reaction, metathesis reaction, etc.
  • the two enantiomers produced may be separated. Any technique known in the art may be used to separate the enantiomers (e.g., crystallization, chiral chromatography, conversion to a diastereomer followed by conventional purification techniques, chiral resolution using an enzyme, chiral resolution via diastereomeric salt crystallization, etc. ). In certain embodiments, a chiral resolution is used. In certain embodiments, a lipase-catalyzed chiral resolution is used. The lipase selectively acetylates one enantiomer versus the other.
  • Any technique known in the art may be used to separate the enantiomers (e.g., crystallization, chiral chromatography, conversion to a diastereomer followed by conventional purification techniques, chiral resolution using an enzyme, chiral resolution via diastereomeric salt crystallization, etc. ).
  • a chiral resolution is used.
  • Amano Lipase AK in the presence of vinyl acetate is used to acetylate preferentially the ( R )-enantiomer.
  • the resulting products i.e., free alcohol versus acetylated alcohol
  • chiral chromatography is used to separate the enantiomers of 11.
  • a particular enantiomer is crystallized, optionally with a chiral salt as a diastereomeric salt.
  • the resulting ( S )-isomer is reacted with a nucleophile to preserve the stereochemistry at the chiral center and yield compound 13.
  • two substitution reactions based on an S N 2 mechanism are used in sequence to preserve the overall stereochemistry at the chiral center.
  • the allylic alcohol is converted to the corresponding bromide with CBr 4 and PPh 3 via an S N 2 mechanism, thereby inverting the stereochemistry at the chiral center.
  • the reaction is accomplished using N -chlorosuccinimide (NCS) or N -bromosuccinimide (NBS) and methyl sulfide.
  • NCS N -chlorosuccinimide
  • NBS N -bromosuccinimide
  • Other reactions for the formation of alkyl halides from allylic alcohols may also be used.
  • reaction conditions of the second substitution reaction also favor an S N 2 reaction so that the stereochemistry at the chiral center is inverted again, thus preserving the overall stereochemistry.
  • nucleophile, leaving group, reagents, solvent, concentration of reagents, temperature, time of reaction, etc. in the above reactions may be adjusted to favor the desired stereochemical outcome, to improve the yield, and/or to adjust other aspects of the reaction.
  • the ( R )-isomer is simply reacted with a nucleophile under reaction conditions that favor an S N 2 mechanism in order to invert the stereochemistry at the chiral center.
  • the alcohol is first converted into a better leaving group (e.g., by forming the corresponding tosylate, mesylate) before reaction with the nucleophile.
  • the nucleophile, leaving group, reagents, solvent, concentration of reagents, temperature, time of reaction, etc. in the above reaction may be adjusted to favor the desired stereochemical outcome and/or to improve the yield.
  • the stereochemistry is preferably as shown in isoxazole 13 of formula:
  • R 5 is -N(R E ) 2 .
  • R 5 is -N(R E ) 2 , wherein R E is C 1 -C 6 alkyl.
  • R 5 is -N(CH 3 ) 2 .
  • R 5 is -OR E .
  • R 5 is -OCH 3 .
  • R 5 is-SR E .
  • R 5 is -SCH 3 .
  • R 5 is acyl.
  • R 5 is substituted or unsubstituted aliphatic or heteroaliphatic.
  • R 5 is -CN, -NO 2 , or halogen.
  • the opposite stereochemistry of 13, that is, may be desired and produced by modifying the above methodology.
  • isoxazole 13, whether of the ( R )- or ( S )-configuration, is an enantiomerically pure compound.
  • isoxazole 13 is at least 80%, 90%, 95%, 98%, or 99% enantiomerically pure. Rather than purifying or resolving the enantiomers of the alcohol in the previous step, it will be appreciated that the purification of the enantiomers may take place after the preparation of isoxazole 13.
  • this separation of two enantiomers may be accomplished by any technique known in the art including, but not limited to, crystallization, chiral chromatography, conversion to a diastereomer followed by conventional purification techniques, chiral resolution using an enzyme, and chiral resolution via diastereomeric salt crystallization.
  • the prepartion of isoxazole 13 is not stereoselective.
  • the desired stereoisomer is separated from the undesired stereoisomer.
  • the undesired stereoisomer may be discarded or converted into the desired stereoisomer or another intermediate useful in the synthesis.
  • the undesired stereoiomer is converted into the desired stereoisomer.
  • isoxazole 13 is metalated and reacted with 3-methoxyfurfural or another substituted furfural moiety.
  • the furfural moiety has a protected hydroxyl group at C-3.
  • an at least 90% enantiomerically pure mixture of isoxazole 13 is used in this reaction.
  • isoxazole 13 is at least 95%, 98%, or 99% enantiomerically pure.
  • isoxazole 13 is reacted with n-butyl lithium, another organolithium reagent, or another metal reagent.
  • a 3-substituted 3-alkoxyoyfurfural or a 4-substituted 3-alkoxyfurfural is used in the reaction.
  • the furfural is a 2- or 4-substituted 3-methoxyfurfural.
  • the furfural moiety is of the formula: wherein
  • the coupling of the isoxazole to the furfural moiety may be achieved using a metal-halogen exchange reaction.
  • an isoxazole of formula: wherein R 3 , R 4 , R 5 , and P are as defined herein; and X is a halogen is used.
  • X is bromine.
  • X is iodine.
  • a magnesium-halogen exchange is used.
  • isoxazole 13a is reacted with i -PrMgCl and then allowed to react with the furfural moiety as described above.
  • the reaction is performed at approximately 0 °C - -20 °C in THF or another suitable solvent.
  • a magnesium-halogen exchange reaction eliminates the need for using highly reactive lithium reagents.
  • other metal-halogen exchange reactions may be used to produce 14 such as a lithium-halogen exchange reaction.
  • the isoxazole of formula 13a may be prepared by direct electrophilic halogenation (e.g ., iodination, bromination) of the alcohol of formula: wherein P is hydrogen or an oxygen protecting group, to yield a halogenated isoxazole of formula: wherein P is defined above, and X is a halogen ( e.g., Br, I). Subsequent oxidation of the primary alcohol (for example, using TEMPO, NaOCl, CH 2 Cl 2 ) followed by addition of a vinyl moiety yields the bromo allylic alcohol of formula: wherein R 3 , R 4 , P, and X are defined herein.
  • direct electrophilic halogenation e.g ., iodination, bromination
  • P is hydrogen or an oxygen protecting group
  • the addition of the vinyl moiety is enantioselective.
  • the enantioselective addition of the vinyl group is accomplished using divinyl zinc and a chiral aminoalcohol ligand.
  • Other suitable chiral aminoalcohols are described herein.
  • the chiral ligand used is an amino-alcohol ligand of formula: The bromo allylic alcohol, or corresponding mesylate or other suitable leaving group, is then displaced to provide: wherein R 3 , R 4 , R 5 , P, and X are defined herein.
  • R 3 , R 4 , R 5 , P, and X are defined herein.
  • Intramolecular Diels-Alder of 14 yields the bridged tricyclic product 15.
  • the Diels-Alder reaction is stereoselective and regioselective yielding only the stereoisomer and regioisomer shown.
  • the desired stereoisomer is at least 80%, 90%, 90%, 98%, or 99% of the product.
  • the desired product is optionally separated from an undesired product or starting material at this stage.
  • the Diels-Alder reaction is catalyzed or uncatalyzed. In certain embodiments, the reaction is uncatalyzed. In certain embodiments, the reaction is catalyzed with a Lewis acid catalyst.
  • the reaction is caused by heating the starting material 14.
  • the compound is heated to a temperature above 60 °C, 70 °C, 80 °C, 90 °, 100 °C, 110 °C, or 120 °C.
  • compound 13 is heated to approximately 115 °C in an organic solvent such as toluene.
  • an organic solvent such as toluene.
  • the free alcohol is oxidized to the corresponding ketone.
  • Any method known in the art for oxidizing a secondary alcohol may be used. Secondary alcohols may be oxidized to the corresponding ketone using oxidizing agents, dehydrogenation, or hypervalent iodine reagents (e.g ., Dess-Martin periodinane). In general, milder oxidizing reagents are used. In certain embodiments, a Swern oxidation is used. In certain embodiments, tetrapropylammonium perruthenate (TPAP)/ N- methylmorpholine- N -oxide (NMO) is used as the oxidizing agent. In certain other embodiments, the free alcohol is protected with an oxygen protecting group rather than oxidizing it to the corresponding ketone. Any oxygen protecting group may be used including silicon-containing protecting groups.
  • the next step involves the removal of the oxygen protecting group P' and rearrangement of the resulting enolate to form the enone 17.
  • the reaction conditions used to remove the protecting group will depend on the particular protecting group being used to mask the enolate.
  • P' is methyl or another alkyl group. Removal of the methyl group with a Lewis acid results in rearrangement of the resulting enolate.
  • the demethylation reaction is performed using BBr 3 .
  • the reaction with BBr 3 is typically performed at approximately -78 °C.
  • the demethylation reaction is performed using BCl 3 .
  • the reaction with BCl 3 is typically performed at approximately -40 °C.
  • BCl 3 can be used at a higher temperature than BBr 3 .
  • other protecting groups can be removed under conditions suitable to selectively remove P' and not affect other functional groups of the enone.
  • the resulting free hydroxyl group of enone 17 is then optionally protected to yield enone 9.
  • the protecting group can be any oxygen protecting group.
  • the oxygen protecting group is a silicon-containing protecting group.
  • the oxygen protecting group is TBS.
  • each of the steps in the synthesis of the enone may be optionally followed by the appropriate work-up and purification of the desired product. Certain steps, however, may not require purification before being used as starting material in the next reaction.
  • the inventive synthesis of the enone may be used to prepare multi-gram quantities. In certain embodiments, at least 25 grams of the enone is prepared. In other embodiments, at least 50 grams of the enone is prepared using the inventive synthesis. In certain other embodiments, at least 100 grams of the enone is prepared.
  • Polycyclic toluates may be used in the Michael-Dieckmann reaction sequence to form pentacyclines, hexacyclines, or higher cyclines.
  • Toluates (not claimed) useful in preparing pentacyclines are exemplified by the formula: wherein
  • Enone (18) may be reacted with an anion (not claimed), which is generated through metalation (e.g ., metal-halogen exchange, metal-metalloid exchange, lithium-halogen exchange, lithium-tin exchange, etc. by reacting the toluate with the appropriate metal reagent) of a toluate of the following formula: wherein
  • any metal may be used in the metalation reaction to generate the metal anionic reagent to be reacted with the enone.
  • the metal is a Group I element on the periodic chart.
  • the metal is a Group II element on the periodic chart.
  • the metal is a transition metal.
  • Exemplary metals useful in the metalation reaction include sodium, lithium, calcium, aluminium, cadmium, copper, beryllium, arsenic, antimony, tin, magnesium, titanium, zinc, manganese, iron, cobalt, nickel, zinc, platinum, palladium, mercury, and ruthenium.
  • the metal is chosen from lithium, magnesium, titanium, zinc, and copper.
  • the metal is magnesium, lithium, sodium, beryllium, zinc, mercury, arsenic, antimony, or tin.
  • a lithium-halogen exchange is used.
  • the lithium-halogen exchange may be performed in situ in the presence of the enone.
  • the lithium-halogen exchange may be preformed using any lithium reagent including, for example, alkyllithium reagents, n -butyllithium, t -butyllithium, phenyl lithium, mesityl lithium, and methyllithium.
  • other organometallics reagents are generated and reacted with the enone.
  • the metal reagent is a magnesium reagent including, but not limited to, magnesium metal, magnesium anthracene, activated magnesium turnings, etc.
  • the reagent is zinc-based.
  • the reagent may be generated in situ in the presence of the enone, or the reagent may be generated separately and later contacted with the enone.
  • milder conditions for the cyclization are used (e.g., a zinc reagent).
  • the toluate may be further substituted in certain embodiments.
  • the phenyl ring of the toluate may be substituted for an aromatic heterocyclic ring or ring system such as a pyridine ring.
  • carbocyclic and heterocyclic analogs of toluate include: (not claimed).
  • the halogen Y is bromine.
  • Y is iodine.
  • Y is chloride.
  • Y is a metalloid (e.g ., tin, selenium, tellurium, etc .).
  • Y is -SnR 3 , wherein each occurrence of R is independently alkyl ( e.g., -Sn(CH 3 ) 3 ). After the metalation reaction, Y is a metal such as lithium, magnesium, zinc, copper, antimony, sodium, etc.
  • R 1 is hydrogen or lower alkyl (C 1 -C 6 ). In certain particular embodiments, R 1 is hydrogen.
  • Polycyclic toluates may be used to prepare pentacyclines, hexacyclines, or higher cyclines (not claimed).
  • Toluates useful in the preparation of such cyclines are of the formula: wherein
  • the enone (18) may be reacted with a benzocyclobutenol in an o-quinone dimethide Diels-Alder reaction (not claimed).
  • the enone (18) is reacted under suitable conditions (e.g ., heat) with a benzocyclobutenol of formula: wherein
  • the enone may be reacted with an anion of a phthalide or cyano-phthalide.
  • the enone (18) is reacted under basic conditions (e.g. , LDA, Ph 3 CLi) with the anion of the phthalide of formula: wherein
  • the products of the above reactions are optionally further functionalized, reduced, oxidized, rearranged, protected, and deprotected to yield the final desired product.
  • Each of the above steps may be followed with an appropriate work-up and purification of the desired product.
  • various isolation and purification techniques including flash chromatography, crystallization, distillation, HPLC, thin layer chromatography, extraction, filtration, etc. may be used in the course of synthesizing compounds of the invention. These techniques may be used in the preparation or purification of intermediates, reagents, products, starting materials, or solvents.
  • the invention also provides useful intermediates useful in the preparation of the enone (9) and tetracycline analogs.
  • the invention provides a compound of formula (VIII) : wherein
  • the invention provides a compound of formula ( VII ): wherein
  • the invention provides a compound of formula ( IIIb ): wherein
  • the compound is of formula ( II ): wherein
  • tetracycline analogs including, but not limited to, tetracyclines, heterocyclic tetracycline analogs, dicyclines, tricyclines, pentacyclines, heterocylic pentatcyclines, bridged pentacyclines, heterocyclic polycyclines, bridged polycyclines, and other polycyclines, as described in U.S. patent application US 2005/0282787, published on December 22, 2005 ; PCT application WO 05/112945, published December 1, 2005 ; and U.S. provisional patent application, USSN 60/790,413, filed April 7, 2006 .
  • any of the genera, classes, subclasses, or species described in these application may be prepared using the inventive system.
  • Particularly useful compounds of the present invention include those with biological activity.
  • the compounds of the invention exhibit antimicrobial activity.
  • the compound may have a mean inhibitory concentration, with respect to a particular bacteria, of less than 100 ⁇ g/mL, of less than 50 ⁇ g/mL, preferably less than 25 ⁇ g/mL, more preferably less than 5 ⁇ g/mL, and most preferably less than 1 ⁇ g/mL or less than 0.1 ⁇ g/mL.
  • infection caused by the following organisms may be treated with antimicrobial compounds of the invention: Gram-positivives -Staphylocococcus aureus, Staphylococcus epidermidis, Streptococcus Group A, Streptococcus viridans, Streptococcus pneumoniae, Enterococcus faecalis; Gram-negatives- Neisseria meningitidis, Neisseria gonorrhoeae, Haemophilus influenzae, Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii, Bacteroides fragilis, other Bacteroides; and others -Mycoplasma pneumoniae, Treponema pallidum, Rickettsia, and Chlamydia.
  • the compounds exhibit anti-fungal activty.
  • the compounds of the invention exhibit antiproliferative activity.
  • Analytical thin-layer chromatography was performed using glass plates pre-coated with 0.25 mm 230-400 mesh silica gel impregnated with a fluorescent indicator (254 nm). Thin layer chromatography plates were visualized by exposure to ultraviolet light and/or exposure to ceric ammonium molybdate or an acidic solution of p -anisaldehyde followed by heating on a hot plate.
  • Chlorotrimethylsilane, triethylamine, diisopropylamine, 2,2,6,6-tetramethylpiperidine, N,N, N' ; N' -tetramethylethylenediamine, DMPU, HMPA, and N,N- diisopropylethylamine were distilled from calcium hydride under dinitrogen atmosphere.
  • n -butyllithium, s -butyllithium, and t -butyllithium were determined by titration with a tetrahydrofuran solution of 2-butanol using triphenylmethane as an indicator ( Duhamel, L.; Palquevent, J.-C. J. Org. Chem. 1979, 44, 3404-3405 ).
  • IR Infrared
  • Optical rotations were determined on a JASCO DIP-370 digital polarimeter equipped with a sodium lamp source using a 200- ⁇ L or 2-mL solution cell. High resolution mass spectra were obtained at the Harvard University Mass Spectrometry Facilities.
  • Amano Lipase AK (125 mg) was added to a mixture of allylic alcohol 2 (1.00 g, 4.30 mmol, 1 equiv), 4 ⁇ molecular sieves (65 mg), and vinyl acetate (3.40 mL, 36.9 mmol, 8.57 equiv) in hexanes (17 mL) at 23 °C. After stirring for 52.5 h, the reaction mixture was filtered and the filtrate was concentrated.
  • Methanesulfonyl chloride (589 ⁇ L, 7.46 mmol, 1.15 equiv) was added dropwise via syringe to a solution of alcohol JDB5 (1.50 g, 6.49 mmol, 1 equiv) and triethylamine (1.18 mL, 8.44 mmol, 1.30 equiv) in dichloromethane (65 mL) at -10 °C. After stirring at -10 °C for 40 min, the reaction mixture was cooled to -30 °C and a solution of dimethylamine in tetrahydrofuran (5.30 M, 7.40 mL, 38.9 mmol, 6.00 equiv) was added via syringe.
  • reaction mixture was allowed to warm slowly to 5 °C over 4.5 h, then was partitioned between aqueous potassium phosphate buffer (pH 7.0, 0.05 M, 50 mL) and dichloromethane (100 mL). The aqueous layer was further extracted with dichloromethane (50 mL). The organic layers were combined and the combined layers were washed with saturated aqueous sodium chloride solution (50 mL). The washed solution was dried over sodium sulfate and the solids were filtered.
  • the residue obtained was purified by flash-column chromatography on silica gel (50% diethyl ether-pentane, grading to 75% diethyl ether-pentane) to furnish the furyl alcohol JDB7 (626 mg, 84%) as a clear, colorless oil.
  • reaction solution was stirred at -78 °C for 25 min and then triethylamine (1.14 mL, 8.15 mmol, 5.00 equiv) was added.
  • the reaction solution then was allowed to warm to -45 °C over 45 min and saturated aqueous sodium bicarbonate solution (5 mL) was added.
  • the product solution was partitioned between aqueous potassium phosphate buffer (pH 7.0, 0.05 M, 20 mL) and dichloromethane (50 mL). The aqueous layer was further extracted with dichloromethane (25 mL). The organic layers were combined and the combined layers were dried over sodium sulfate. The solids were filtered and the filtered solution was concentrated.
  • reaction solution was stirred at 23 °C for 65 min, then was partitioned between aqueous potassium phosphate buffer (pH 7.0, 0.05 M, 20 mL) and dichloromethane (40 mL). The aqueous layer was separated and further extracted with dichloromethane (20 mL). The organic layers were combined and the combined layers were dried over sodium sulfate. The solids were filtered and the filtrate was concentrated.
  • TLC plates were visualized by exposure to ultraviolet light (UV), and then were stained by submersion in aqueous ceric ammonium molybdate solution (CAM), basic aqueous potassium permanganate (KMnO 4 ), or an acidic solution of p -anisaldehyde in ethanol, followed by brief heating on a hot plate ( ⁇ 170 °C, 10-15 s). Flash-column chromatography was performed as described by Still et al. (J. Org. Chem. 1978, 43, 2923 ), employing silica gel (60- ⁇ pore size, 32-63 ⁇ m, standard grade, Sorbent Technologies).
  • the reaction mixture was filtered, and the filtrate was washed with water (100 mL).
  • the washed product solution was then extracted into aqueous citric acid solution (30% by weight, 2 x 200 mL).
  • the citric acid layers were combined, cooled in an ice-water bath, and brought to pH 13 by slow addition of aqueous sodium hydroxide solution (6 N).
  • the basic aqueous mixture was extracted with toluene (3 x 300 mL).
  • the toluene layers were combined and washed sequentially with water (200 mL) and saturated aqueous sodium chloride solution (300 mL).
  • the washed solution was dried over sodium sulfate and the solids were filtered.
  • a 5-L, two-necked, round-bottomed flask with a coarse fritted funnel fused at a 45° angle was equipped with a mechanical stirrer.
  • the system was flame-dried, flushed with argon, and charged with a solution of zinc chloride in diethyl ether (1.0 M, 1 L, 1 mol, 1 equiv).
  • a solution of vinylmagnesium bromide in tetrahydrofuran (1.0 M, 2 L, 2 mol, 2 equiv) was added via cannula over 2.5 h.
  • a gray solid precipitated throughout the addition The reaction mixture was stirred at 23 °C for 2 h, and then dioxane (600 mL) was added via cannula.
  • the reaction mixture was stirred at 23 °C for an additional 1h.
  • a 3-L, one-necked, flame-dried flask was attached to the joint at the end of the funnel and the mechanical stirrer was replaced by a glass stopper.
  • the entire apparatus was then turned 135° to allow the reaction mixture to filter into the 3-L flask to furnish a yellow solution of divinylzinc (assumed to be 0.28M, 2.25 L).
  • the divinylzinc solution could be used directly in the next reaction, or stored at -20 °C for 2 months with no loss in yield or enantioselectivity during the enantioselective addition described below.
  • N,N- diisopropylethylamine (88.5 mL, 508 mmol, 2.00 equiv) was added, the flask was equipped with a reflux condensor and thermometer, and the reaction mixture was warmed to 95 °C in a heating mantle. After stirring for 105 h, the reaction mixture was warmed to 110 °C for 23 h. The product solution was cooled to 23 °C and loaded directly onto a silica gel plug (14 cm diameter, 17 cm length).
  • the toluene solvent was eluted with 15% acetone-hexanes and then the mixture of Diels-Alder products were eluted by grading to 65% acetone hexanes to give a mixture which was carried on directly to the Swern oxidation (76.6 g, 78%).
  • a 5-L, three-necked, round-bottomed flask was oven-dried and flushed with argon.
  • the flask was equipped with a mechanical stirrer and thermocouple, and then was charged with a solution of oxalyl chloride (24.6 mL, 279 mmol, 1.40 equiv) in dichloromethane (1 L).
  • the solution was cooled to -78°C in a dry ice-acetone bath, and then a solution of dimethyl sulfoxide (35.3 mL, 498 mmol, 2.50 equiv) in dichloromethane (500 mL) was added dropwise over 90 min.
  • the reaction solution was stirred for 10 min and then a solution of Diels-Alder precursors 9-12 (76.6 g, 199 mmol, 1 equiv) in dichloromethane (500 mL) was added dropwise via cannula to the cold reaction solution.
  • the flask containing 9-12 was rinsed with dichloromethane (25 mL) and the rinse solution was transferred to the reaction flask, via cannula.
  • the reaction solution was stirred at -78 °C for 25 min and then triethylamine (139 mL, 995 mmol, 5.00 equiv) was added.
  • reaction solution then was allowed to warm to -65 °C over 80 min and saturated aqueous sodium bicarbonate solution (700 mL) was added.
  • the product solution was partitioned between aqueous potassium phosphate buffer (pH 7.0, 0.05 M, 500 mL) and dichloromethane (750 mL).
  • the aqueous layer was further extracted with dichloromethane (500 mL).
  • the organic layers were combined and the combined layers were dried over sodium sulfate. The solids were filtered and the filtrate was concentrated.
  • the residue obtained was purified by flash-column chromatography on silica gel (30% acetone-hexanes, grading to 50% acetone-hexanes) to furnish the ketone 8 (55.4 g, 73%, single diastereomer) as a pale yellow solid.
  • the exo product was also observed prior to chromatography, but fractions containing that product were discarded.
  • TLC 50% acetone-hexanes
  • R f 0.33 (UV, CAM).
  • a 3-L, one-necked, round-bottomed flask was equipped with a Teflon-coated magnetic stirbar. The system was flame-dried and flushed with argon. The flask was charged with a solution of N , N -dimethylformamide (31.9 mL, 413 mmol, 1.35 equiv) in dichloromethane (1.2 L). The solution was cooled to 0 °C in a dry ice-acetone bath, and then oxalyl chloride (32.5 mL, 367 mmol, 1.2 equiv) was added over 16 min. Vigorous bubbling occurred and a white solid precipitated.
  • a 200-mL, one-necked, round-bottomed flask was equipped with a Teflon-coated magnetic stirbar and flame-dried.
  • the flask was charged with a solution of isoxazole 5 (2.00 g, 7.75 mmol, 1 equiv) in tetrahydrofuran (52 mL).
  • the solution was cooled to -100°C in a liquid dinitrogen-ethanol bath, and then a solution of n -butyllithium in hexanes (2.50 M, 3.56 mL, 8.91 mmol, 1.15 equiv) was added dropwise over 9 min.
  • the reaction solution was warmed to -65 °C over 15 min.
  • the mixture was stirred at -65 °C for 60 min and then a solution of iodine (2.56 g, 10.1 mmol, 1.30 equiv) in tetrahydrofuran (25 mL) was added via cannula.
  • the reaction solution was stirred at -65 °C for 15 min, and then the cooling bath was removed.
  • the product solution was partitioned between aqueous potassium phosphate buffer (pH 7.0, 0.05 M, 25 mL), saturated aqueous sodium thiosulfate solution (25 mL), and ethyl acetate (150 mL).
  • a 5-mL, one-necked, round-bottomed flask was equipped with a Teflon-coated magnetic stirbar flame-dried.
  • the flask was charged with a solution of iodide 13 (49 mg, 0.13 mmol, 1 equiv) in tetrahydrofuran (850 ⁇ L).
  • the solution was cooled to -20 °C in a dry ice-acetone bath, and then a solution of isopropylmagnesium chloride in tetrahydrofuran (2.0 M, 96 ⁇ L, 0.19 mmol, 1.5 equiv) was added dropwise.
  • Fragment coupling of the bromo allylic amine and 3-methoxyfurfural was performed by treatment of the bromo allylic amine with iso -PrMgCl ( Wakefield, B. J. Preparation of Organomagnesium Compounds. In Organomagnesium Compounds in Organic Synthesis; Academic Press, Inc.: San Diego, 1995 pp 51-59 ; Boudier, A.; Bromm, L. O.; Lotz, M.; Knochel, P. Angew. Chem., Int. Ed. Engl.
  • the reaction mixture was stirred for 60 min, then saturated aqueous sodium thiosulfate (15 mL) was added.
  • the product solution was partitioned between ethyl acetate (75 mL) and aqueous potassium phosphate buffer solution (pH 7.0, 0.05 M, 20 mL).
  • the aqueous layer was extracted with ethyl acetate (50 mL).
  • the organic layers were combined and the combined solution was washed with saturated aqueous sodium chloride solution (50 mL). The washed solution was dried over sodium sulfate, the solids were filtered, and the filtrate was concentrated.
  • Aqueous sodium hypochlorite solution (21.8 mL, 0.83 M, 18.1 mmol, 1.2 equiv) was then added to the biphasic mixture.
  • the red biphasic mixture was stirred for 15 min, then saturated aqueous sodium thiosulfate solution (75 mL) was added.
  • the product solution was partitioned and the aqueous layer was further extracted with dichloromethane (150 mL). The organic layers were combined and the combined solution was dried over sodium sulfate. The solids were filtered, and the filtrate was concentrated.
  • the solution was cooled to 0 °C in an acetone bath, and a solution of n -butyllithium in hexanes (2.50 M, 2.10 mL, 5.31 mmol, 2.00 equiv) was added to the cooled solution via syringe.
  • the reaction solution was stirred for an additional 30 min at 0 °C after the addition, and then a solution of divinylzinc (0.28 M, prepared as described above, 19.0 mL, 5.31 mmol, 2.0 equiv) was added via syringe over 5 min.
  • the reaction mixture was stirred at 0 °C for 1 h, then was cooled to an internal temperature of-75 °C by addition of dry ice to the cooling bath.
  • a 10-mL, single-necked, round-bottomed flask equipped with a Teflon-coated magnetic stirring bar was flame-dried, then flushed with argon.
  • the flask was charged with a solution of alcohol 212 (128 mg, 0.413 mmol, 1 equiv) in dichloromethane (1.37 mL).
  • the solution was cooled to -15 °C and triethylamine (81 ⁇ L, 0.58 mmol, 1.4 equiv) and methanesulfonyl chloride (39 ⁇ L, 0.50 mmol, 1.2 equiv) were added sequentially.
  • reaction mixture was stirred at -15 °C for 15 min, then was cooled to -45 °C.
  • 2,2,2-Trifluoroethanol (281 ⁇ L, 3.72 mmol, 9.00 equiv) and a solution of dimethylamine (3.6 M in CH 2 Cl 2 , 800 ⁇ L,, 2.9 mmol, 7.0 equiv) were added sequentially and the reaction mixture was stirred at -30 °C for 92 h.
  • the product solution was warmed to 23 °C and partitioned between dichloromethane (15 mL) and aqueous potassium phosphate solution (pH 7.0, 0.05 M, 5 mL).
  • a 5-mL, single-necked, round-bottomed flask equipped with a Teflon-coated magnetic stirring bar was flame-dried, then flushed with argon.
  • the flask was charged with a solution of bromide 213 (61 mg, 0.18 mmol, 1 equiv) in tetrahydrofuran (904 ⁇ L).
  • the solution was cooled to 0 °C in an ice-water bath, then a solution of isopropylmagnesium chloride in tetrahydrofuran (2.0 M, 180 ⁇ L, 0.36 mmol, 2.0 equiv) was added dropwise.
  • the residue obtained was purified by flash-column chromatography on silica gel (70% ethyl ether-pentane) to furnish the Diels-Alder precursors 182 (69 mg, 99%, 1.4:1 mixture of epimers) as a pale yellow oil.
  • the product provided spectroscopic data identical to those presented above save for differences attributable to the varying ratio of product diastereomers.
  • the method further comprising the step of protecting the hydroxyl group of the enone of formula ( VIII ) to yield an enone of formula ( IX ) wherein P' is an oxygen-protecting group.
  • Method 3 can further comprise the steps of:
  • Method 4 can further comprise the step of deprotecting the product of formula: to yield a tetracycline of formula:
  • Method 3 can further comprise the step of:
  • Method 6 can further comprise the step of deprotecting the product of formula: to yield a tetracycline of formula:
  • Method 3 can further comprise step of:
  • Method 8 can further comprise the step of deprotecting the product of formula: to yield a tetracycline of formula:
  • Method 3 can further comprise the step of reacting an enone ( IX ) under suitable conditions with a diene of formula (not claimed): wherein
  • Method 10 can further comprise the step of deprotecting the product of formula: to yield a tricycline of formula:
  • Method 3 can further comprise reacting an anion of the phthalide of formula (not claimed): wherein
  • Method 12 can further comprise the step of deprotecting the product of formula: to yield a tetracycline of formula:
  • P' can be a silyl-protecting group or P' is t -butyldimethylsilyl.
  • P can be benzyl.
  • R 3 can be hydrogen or C 1 -C 6 alkyl or methyl or -OR C .
  • R 4 can be hydrogen or C 1 -C 6 alkyl or methyl or -OR D .
  • R 5 can be -N(CH 3 ) 2 or -N(R E ) 2 or-OR E or -SR E .
  • P' can be methyl.
  • the suitable condition may include the presence of BBr 3 or BCl 3 .
  • P' can be methyl.
  • the step of oxidizing comprises a Swern oxidation.
  • the step of adding can comprise reacting the compound of formula ( III ) with a metal reagent or base.
  • the metal reagent can be a lithium reagent.
  • the lithium reagent can be n -BuLi.
  • the step of adding can comprise reacting the compound of formula ( III ) with a metal reagent.
  • the metal reagent can a magnesium reagent.
  • the lithium reagent can be i- PrMgCl.
  • the step of substituting can result in a retention of stereochemistry at the carbon atom to which R 5 is attached.
  • the step of substituting can comprise: converting the hydroxyl group to a leaving group, wherein the step of converting results in an inversion of stereochemistry; and substituting the leaving group with a nucleophile, wherein the step of substituting results in a second inversion of stereochemistry.
  • the leaving group can be a halide.
  • the halide can be a bromide.
  • the step of substituting can result in an inversion of stereochemistry at the carbon atom to which R 5 is attached.
  • P' can be acetyl, or mesylate (Ms) or tosylate (Ts).
  • the step of substituting can comprise: deprotecting the acetylated hydroxyl group of formula ( IIb ), wherein P' is acetyl; converting the unprotected hydroxyl group into a better leaving group with retention of stereochemistry; and substituting the leaving group with a nucleophile.
  • the better leaving group can be -OMs.
  • the lipase can be Amano Lipase AK.
  • the suitable conditions can comprise the presence of vinyl acetate.
  • R 3 and R 4 can both be hydrogen.
  • P can be benzyl.
  • the vinyl reagent can be a metal vinyl reagent.
  • the vinyl reagent can be
  • R 3 and R 4 can both be hydrogen.
  • P can be benzyl.
  • the vinyl reagent can be a metal vinyl reagent.
  • the vinyl reagent can be divinyl zinc.
  • the vinyl reagent can be divinyl zinc in the presence of a chiral ligand of formula:
  • R 3 can be hydrogen.
  • R 4 can be hydrogen.
  • R 3 and R 4 can both hydrogen.
  • At least one of R 3 and R 4 can be C 1 -C 6 alkyl.
  • R 5 can be -N(R E ) 2 or-N(CH 3 ) 2 .
  • P can be benzyl.
  • P" can be hydrogen.
  • P' can be methyl.
  • X can be hydrogen, or iodine, or bromine. Both R 3 and R 4 can be hydrogen. P' can b hydrogen.
  • P' can be hydrogen, or acetyl or P' is tosylate (Ts) or P' is mesylate (Ms).
  • the compound can have the stereochemistry shown in formula ( IIb ): or the stereochemistry shown in formula ( IIa ):

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Claims (15)

  1. Procédé de préparation d'un composé de formule :
    Figure imgb0235
     ou un sel, tautomère, stéréoisomère, énantiomère ou diastéréoisomère de celui-ci ; dans lequel :
    R1 est hydrogène ; halogène ; aliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; hétéroaliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; acyle substitué ou non substitué, ramifié ou non ramifié ; aryle substitué ou non substitué ; hétéroaryle substitué ou non substitué ; -ORA ; -C(=O)RA ; -CO2RA ; -CN ; -SCN ; -SRA ; -SORA ; -SO2RA ; -NO2 ; -N(RA)2 ; -NHC(O)RA ; ou -C(RA)3 ; où chaque occurrence de RA est indépendamment hydrogène, un groupe protecteur, aliphatique, hétéroaliphatique, acyle, aryle, hétéroaryle, alcoxy, aryloxy, alkylthio, arylthio, amino, alkylamino, dialkylamino, hétéroaryloxy ou hétéroarylthio ;
    R2 est hydrogène ;
    R3 est hydrogène ; halogène ; aliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; hétéroaliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; acyle substitué ou non substitué, ramifié ou non ramifié ; aryle substitué ou non substitué ; hétéroaryle substitué ou non substitué ; -ORC ; =O (conjointement avec R4) ; -C(=O)RC ; -CO2RC ; -CN ; -SCN ; -SRC ; -SORC ; -SO2 RC ; -NO2 ; -N(RC)2 ; -NHC(O)RC ; ou -C(RC)3 ; où chaque occurrence de RC est indépendamment hydrogène, un groupe protecteur, aliphatique, hétéroaliphatique, acyle, aryle, hétéroaryle, alcoxy, aryloxy, alkylthio, arylthio, amino, alkylamino, dialkylamino, hétéroaryloxy ou hétéroarylthio ;
    R4 est hydrogène ; halogène ; aliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; hétéroaliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; acyle substitué ou non substitué, ramifié ou non ramifié ; aryle substitué ou non substitué ; hétéroaryle substitué ou non substitué ; -ORD ; =O (conjointement avec R3) ; -C(=O)RD ; -CO2RD ; -CN ; -SCN ; -SRD ; -SORD ; -SO2 RD ; -NO2 ; -N(RD)2 ; -NHC(O)RD ; ou -C(RD)3 ; où chaque occurrence de RD est indépendamment hydrogène, un groupe protecteur, aliphatique, hétéroaliphatique, acyle, aryle, hétéroaryle, alcoxy, aryloxy, alkylthio, arylthio, amino, alkylamino, dialkylamino, hétéroaryloxy ou hétéroarylthio ;
    R5 est hydrogène ; halogène ; aliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; hétéroaliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; acyle substitué ou non substitué, ramifié ou non ramifié ; aryle substitué ou non substitué ; hétéroaryle substitué ou non substitué ; -ORE ; -CN ; -SCN ; -SRE ; ou -N(RE)2 ; où chaque occurrence de RE est indépendamment hydrogène, un groupe protecteur, aliphatique, hétéroaliphatique, acyle, aryle, hétéroaryle, alcoxy, aryloxy, alkylthio, arylthio, amino, alkylamino, dialkylamino, hétéroaryloxy ou hétéroarylthio ;
    R7 est hydrogène ; halogène ; aliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; hétéroaliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; acyle substitué ou non substitué, ramifié ou non ramifié ; aryle substitué ou non substitué ; hétéroaryle substitué ou non substitué ; -ORG ; -C(=O)RG ; -CO2RG ; -CN ; -SCN ; -SRG ; -SORG ; -SO2RG ; -NO2 ; -N(RG)2 ; -NHC(O)RG ; ou -C(RG)3 ; où chaque occurrence de RG est indépendamment hydrogène, un groupe protecteur, aliphatique, hétéroaliphatique, acyle, aryle, hétéroaryle, alcoxy, aryloxy, alkylthio, arylthio, amino, alkylamino, dialkylamino, hétéroaryloxy ou hétéroarylthio ;
    et
    n est un entier dans la plage de 0 à 3, inclus ;
    le procédé comprenant les étapes de :
    (1) fourniture d'une cétone de formule (VII) :
    Figure imgb0236
     ou un sel, tautomère, stéréoisomère, énantiomère, ou diastéréoisomère de celle-ci ; dans laquelle :
    R6 est hydrogène ;
    P est hydrogène ou un groupe protecteur d'oxygène ; et P' est hydrogène, alkyle en C1-C6, acyle, ou un groupe protecteur d'oxygène ;
    (2) déprotection de l'énolate de la cétone (VII) dans des conditions adaptées pour conduire à un réarrangement pour obtenir une énone de formule (VIII) :
    Figure imgb0237
     ou un sel, tautomère, stéréoisomère, énantiomère, ou diastéréoisomère de celle-ci ;
    (3) protection du groupe hydroxyle de l'énone de formule (VIII) pour obtenir une énone de formule (IX) :
    Figure imgb0238
     ou un sel, tautomère, stéréoisomère, énantiomère, ou diastéréoisomère de celle-ci ;
    dans laquelle P" est un groupe protecteur d'oxygène.
    (4) déprotonation d'un toluate de formule :
    Figure imgb0239
     dans des conditions basiques pour produire un anion du toluate ; dans lequel :
    R9 est -OR1 ; -CN ; -SCN ; -SR1 ; ou -N(R1)2 ; où chaque occurrence de R1 est indépendamment hydrogène, un groupe protecteur ; un aliphatique cyclique ou acyclique, substitué ou non substitué ; un hétéroaliphatique cyclique ou acyclique, substitué ou non substitué ; un aryle substitué ou non substitué ; ou un hétéroaryle substitué ou non substitué ; et P"' est hydrogène, un groupe alkyle en C1-C6, un groupe acyle ou un groupe protecteur d'oxygène ;
    (5) réaction de l'anion du toluate avec l'énone (IX) pour former le produit de formule :
    Figure imgb0240
     ou un sel, tautomère, stéréoisomère, énantiomère, ou diastéréoisomère de celui-ci ; et
    (6) déprotection du produit pour obtenir une tétracycline de formule :
    Figure imgb0241
  2. Procédé de la revendication 1, dans lequel R1 est hydrogène.
  3. Procédé de la revendication 1, dans lequel R3 et R4 sont hydrogène.
  4. Procédé de la revendication 1, dans lequel R5 est -N(RE)2, de préférence dans lequel R5 est -N(CH3)2.
  5. Procédé de la revendication 1, dans lequel R7 est halogène ; aliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; hétéroaliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; acyle substitué ou non substitué, ramifié ou non ramifié ; aryle substitué ou non substitué ; hétéroaryle substitué ou non substitué ; -ORG ; -C(=O)RG ; -CO2RG ; -CN ; -SCN ; -SRG ; -SORG ; -SO2RG ; -NO2 ; -N(RG)2 ; -NHC(O)RG ; ou -C(RG)3, et n est un entier autre que 0.
  6. Procédé de la revendication 1, dans lequel la déprotection de l'énolate de la cétone (VIII) dans des conditions adaptées comprend l'utilisation de BBr3 ou BCl3.
  7. Procédé de résolution d'énantiomères de formule (II) :
    Figure imgb0242
     dans laquelle :
    R3 est hydrogène ; halogène ; aliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; hétéroaliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; acyle substitué ou non substitué, ramifié ou non ramifié ; aryle substitué ou non substitué ; hétéroaryle substitué ou non substitué ; -ORC; -C(=O)RC ; -CO2RC ; -CN ; -SCN ; -SRC ; -SORC ; -SO2RC ; -NO2 ; -N(RC)2 ; -NHC(O)RC ; ou -C(RC)3 ; où chaque occurrence de RC est indépendamment hydrogène, un groupe protecteur, aliphatique, hétéroaliphatique, acyle, aryle, hétéroaryle, alcoxy, aryloxy, alkylthio, arylthio, amino, alkylamino, dialkylamino, hétéroaryloxy ou hétéroarylthio ;
    R4 est hydrogène ; halogène ; aliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; hétéroaliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; acyle substitué ou non substitué, ramifié ou non ramifié ; aryle substitué ou non substitué ; hétéroaryle substitué ou non substitué ; -ORD ; -C(=O)RD ; -CO2RD ; -CN ; -SCN ; -SRD ; -SORD ; -SO2RD ; -NO2 ; -N(RD)2 ; -NHC(O)RD ; ou -C(RD)3 ; où chaque occurrence de RD est indépendamment hydrogène, un groupe protecteur, aliphatique, hétéroaliphatique, acyle, aryle, hétéroaryle, alcoxy, aryloxy, alkylthio, arylthio, amino, alkylamino, dialkylamino, hétéroaryloxy ou hétéroarylthio ; et
    P est hydrogène ou un groupe protecteur d'oxygène ;
    le procédé comprenant :
    (1) la réaction de l'alcool de formule (II) avec une lipase dans des conditions adaptées pour acétyler sélectivement le groupe hydroxyle d'un énantiomère de l'alcool ; et
    (2) facultativement, la séparation de l'alcool acétylé de l'alcool non acétylé.
  8. Procédé de la revendication 8, dans lequel la lipase est Amano Lipase AK.
  9. Procédé de la revendication 8, dans lequel les conditions adaptées comprennent la présence d'acétate de vinyle.
  10. Procédé de préparation d'un composé de formule (II) :
    Figure imgb0243
     dans lequel :
    R3 est hydrogène ; halogène ; aliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; hétéroaliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; acyle substitué ou non substitué, ramifié ou non ramifié ; aryle substitué ou non substitué ; hétéroaryle substitué ou non substitué ; -ORC; -C(=O)RC ; -CO2RC ; -CN ; -SCN ; -SRC ; -SORC ; -SO2RC ; -NO2 ; -N(RC)2 ; -NHC(O)RC ; ou -C(RC)3 ; où chaque occurrence de RC est indépendamment hydrogène, un groupe protecteur, aliphatique, hétéroaliphatique, acyle, aryle, hétéroaryle, alcoxy, aryloxy, alkylthio, arylthio, amino, alkylamino, dialkylamino, hétéroaryloxy ou hétéroarylthio ;
    R4 est hydrogène ; halogène ; aliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; hétéroaliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; acyle substitué ou non substitué, ramifié ou non ramifié ; aryle substitué ou non substitué ; hétéroaryle substitué ou non substitué ; -ORD ; -C(=O)RD ; -CO2RD ; -CN ; -SCN ; -SRD ; -SORD ; -SO2RD ; -NO2 ; -N(RD)2 ; -NHC(O)RD ; ou -C(RD)3 ; où chaque occurrence de RD est indépendamment hydrogène, un groupe protecteur, aliphatique, hétéroaliphatique, acyle, aryle, hétéroaryle, alcoxy, aryloxy, alkylthio, arylthio, amino, alkylamino, dialkylamino, hétéroaryloxy ou hétéroarylthio ; et
    P est choisi dans le groupe constitué d'hydrogène et un groupe protecteur d'oxygène ;
    le procédé comprenant la réduction d'un aldéhyde de formule (I) :
    Figure imgb0244
     avec un réactif vinylique substitué ou non substitué dans des conditions adaptées pour obtenir un alcool de formule :
    Figure imgb0245
  11. Procédé de préparation d'un composé de formule (II) :
    Figure imgb0246
     dans lequel :
    R3 est hydrogène ; halogène ; aliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; hétéroaliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; acyle substitué ou non substitué, ramifié ou non ramifié ; aryle substitué ou non substitué ; hétéroaryle substitué ou non substitué ; -ORC; -C(=O)RC ; -CO2RC ; -CN ; -SCN ; -SRC ; -SORC ; -SO2RC ; -NO2 ; -N(RC)2 ; -NHC(O)RC ; ou -C(RC)3 ; où chaque occurrence de RC est indépendamment hydrogène, un groupe protecteur, aliphatique, hétéroaliphatique, acyle, aryle, hétéroaryle, alcoxy, aryloxy, alkylthio, arylthio, amino, alkylamino, dialkylamino, hétéroaryloxy ou hétéroarylthio ;
    R4 est hydrogène ; halogène ; aliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; hétéroaliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; acyle substitué ou non substitué, ramifié ou non ramifié ; aryle substitué ou non substitué ; hétéroaryle substitué ou non substitué ; -ORD ; -C(=O)RD ; -CO2RD ; -CN ; -SCN ; -SRD ; -SORD ; -SO2RD ; -NO2 ; -N(RD)2 ; -NHC(O)RD ; ou -C(RD)3 ; où chaque occurrence de RD est indépendamment hydrogène, un groupe protecteur, aliphatique, hétéroaliphatique, acyle, aryle, hétéroaryle, alcoxy, aryloxy, alkylthio, arylthio, amino, alkylamino, dialkylamino, hétéroaryloxy ou hétéroarylthio ; et
    P est choisi dans le groupe constitué d'hydrogène et un groupe protecteur d'oxygène ;
    le procédé comprenant :
    la réduction d'un aldéhyde de formule (I) :
    Figure imgb0247
     avec un réactif vinylique substitué ou non substitué dans des conditions adaptées pour obtenir un alcool de formule :
    Figure imgb0248
  12. Procédé de préparation d'un composé de formule (II) :
    Figure imgb0249
     dans lequel :
    X est un halogène ;
    R3 est hydrogène ; halogène ; aliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; hétéroaliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; acyle substitué ou non substitué, ramifié ou non ramifié ; aryle substitué ou non substitué ; hétéroaryle substitué ou non substitué ; -ORC; -C(=O)RC ; -CO2RC ; -CN ; -SCN ; -SRC ; -SORC ; -SO2RC ; -NO2 ; -N(RC)2 ; -NHC(O)RC ; ou -C(RC)3 ; où chaque occurrence de RC est indépendamment hydrogène, un groupe protecteur, aliphatique, hétéroaliphatique, acyle, aryle, hétéroaryle, alcoxy, aryloxy, alkylthio, arylthio, amino, alkylamino, dialkylamino, hétéroaryloxy ou hétéroarylthio ;
    R4 est hydrogène ; halogène ; aliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; hétéroaliphatique cyclique ou acyclique, substitué ou non substitué, ramifié ou non ramifié ; acyle substitué ou non substitué, ramifié ou non ramifié ; aryle substitué ou non substitué ; hétéroaryle substitué ou non substitué ; -ORD ; -C(=O)RD ; -CO2RD ; -CN ; -SCN ; -SRD ; -SORD ; -SO2RD ; -NO2 ; -N(RD)2 ; -NHC(O)RD ; ou -C(RD)3 ; où chaque occurrence de RD est indépendamment hydrogène, un groupe protecteur, aliphatique, hétéroaliphatique, acyle, aryle, hétéroaryle, alcoxy, aryloxy, alkylthio, arylthio, amino, alkylamino, dialkylamino, hétéroaryloxy ou hétéroarylthio ; et
    P est choisi dans le groupe constitué d'hydrogène et un groupe protecteur d'oxygène ; le procédé comprenant :
    (1) la bromation d'un alcool de formule :
    Figure imgb0250
     dans des conditions adaptées pour obtenir un alcool bromé de formule :
    Figure imgb0251
    (2) l'oxydation de l'alcool bromé dans des conditions adaptées pour obtenir un aldéhyde bromé de formule :
    Figure imgb0252
     et
    (3) la réduction de l'aldéhyde bromé avec un réactif vinylique substitué ou non substitué dans des conditions adaptées pour obtenir un alcool de formule :
    Figure imgb0253
  13. Procédé de l'une quelconque des revendications 10 à 12, dans lequel le réactif vinylique est un réactif vinylique métallique.
  14. Procédé de la revendication 11 ou 12, dans lequel la réactif vinylique est divinyl-zinc, de préférence dans lequel le réactif vinylique est divinyl-zinc en présence d'un ligand chiral de formule :
    Figure imgb0254
  15. Procédé de la revendication 10, dans lequel le réactif vinylique est
    Figure imgb0255
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